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For only a few years, it has been possible to resolve biological structures down to the molecular scale with light microscopy, termed super-resolution microscopy. This has led to a number of new insights into biological processes. However, there have been limits to the techniques: so far it has been difficult to distinguish between sample specific and microscope specific error sources if the images were blurry. Moreover, different techniques could not easily be compared. This issue has recently been resolved by the Technical University of Braunschweig.
“In analogy to distance marks on a common ruler, spots with a defined number of fluorescent dye molecules are employed as marks”, the group leader Professor Philip Tinnefeld describes the main principle. The scaffold of these structures is a long circular DNA molecule which is folded in the desired shape by adding hundreds of short complementary DNA staple strands. Millions of these so-called DNA origami structures can be assembled simultaneously in a single step. Depending on the desired application, the structures can be reprogrammed to host various dye molecules at different positions.
With these nanorulers the scientists can now evaluate the performance of microscopes and different microscopy techniques. The rulers can be adjusted to different sensitivities and resolutions of all common optical super-resolution techniques. Especially for the resolution range of 6-200 nm, which has become accessible a few years ago, the nanorulers provide the possibility to compare currently competing microscopy techniques.
COMPAMED.de; Quelle: Technical University of Braunschweig